One??Pot Synthesis of 6??Hydroxyisochromans: The Example of Demethyl??oxa??coclaurine
…, A Bianco, C Marra, C Cavarischia
Index: Guiso, Marcella; Bianco, Armandodoriano; Marra, Carolina; Cavarischia, Claudia European Journal of Organic Chemistry, 2003 , # 17 p. 3407 - 3411
Full Text: HTML
Citation Number: 21
Abstract
Abstract Using a modified oxa-Pictet Spengler reaction that we recently described, we synthesized 6-hydroxy-isochromans and their 7-hydroxy derivatives. The successful one step synthesis did not require protecting groups and provided high yields. The obtainment of 1-(4′-hydroxybenzyl)-6, 7-dihydroxyisochroman (1) indicates that this protocol can be used to synthesize oxygenated analogues of benzyl-tetrahydroisoquinoline alkaloids, such as ...
Related Articles:
Improving process conditions of hydroxytyrosol synthesis by toluene-4-monooxygenase
[Journal of Molecular Catalysis B: Enzymatic, , vol. 84, p. 121 - 127]
Pulsed ultraviolet laser photolysis of substituted phenyl diazosulphonates at 248 nm
[Berichte der Bunsen-Gesellschaft, , vol. 99, # 12 p. 1495 - 1503]